Suitable for the cultivation and drug sensitivity testing of Candida and Cryptococcus neoformans.
Mycoplasma Cultivation/Identification/ Enumeration/ Susceptibility Test Kit is intended for cultivation, identification, enumeration and antibiotic susceptibility tests of Ureaplasma Urealyticum (UU) and Mycoplasma Hominis(MH) in human urogenital tract in one step.
Chlamydia Trachomatis Antigen Test Cassette is a lateral flow immunoassay for the qualitative detection antigen of chlamydia in clinical specimens without other supporting instruments.
The Flu A&B / Covid-19 / RSV / Adenovirus / MP Antigen Rapid Test is a rapid coloured chromatography immunoassay for the simultaneous qualitative
SARS-COV-2 Antigen Rapid Test Device is a rapid visual immunoassay for the qualitative, presumptive detection of SARS-CoV-2 nucleocapsid (N) antigen in human nasal swab specimens.
Easy Operation / Clear Results / Accuracy & Safety / Stable Quality
Gonorrhea+Chlamydia Antigen Combo Test Cassette is a lateral flow immunoassay for the qualitative detection antigen of chlamydia and Gonorrhea in clinical specimens without other supporting instruments.
The Influenza A+B Rapid Test Device is a rapid chromatographic immunoassay for qualitative detection of influenza A and B antigens in nasal swab, throat swab or nasal aspirate specimens.
This product uses antigen-antibody specific reaction and immunochromatographic analysis technology, and can qualitatively detect the presence of Helicobacter pylori antigen in stool without other supporting instruments.
This product is primarily used for the culture, identification, and drug sensitivity testing of Ureaplasma urealyticum (UU) and Mycoplasma hominis (MH) in the urogenital system.
This product is mainly suitable for urogenital tract system ureaplasma Urealyticum (UU), Mycoplasma hominis (MH) for culture, identification, and determination of drug sensitivity.
For one-time use in the isolation and culture of Neisseria gonorrhoeae in medical units.
It is compatible with the specific dry reagent based on fluorescence immunochromatography produced by Zhuhai Encode Medical Engineering Co., Ltd. for the immunofluorescence detection of human samples.
Suitable for drug sensitivity reagents of 26 wells,48 wells,96 wells micro plates from different manufacturers, and can automatically complete the distribution of bacterial liquid and mineral oil.
Urinalysis Reagent Strips are made for urinalysis of both qualitative and semi-quantitative
The Alcohol Rapid Test Strip (Urine) is a rapid, highly sensitive method to detect the presence of alcohol in human urine. This test provides a preliminary result only.
The Alcohol Rapid Test Strip (Saliva) is a rapid, highly sensitive method to detect the presence of alcohol in saliva and provide an approximation of relative blood alcohol concentration.
The Multi-Drug Rapid Test Cassette for multiple drugs and drug metabolites is a lateral flow chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in human oral fluid at the specific cut-off concentrations
The test kit is one of urine test kits that do not need any devices or equipment
This automatic blood culture bottle(biochemical sensor) is used for culture in vitro and detection of microorganisms in human blood or other sterile body fluid under normal condition.
This automatic blood culture bottle(biochemical sensor) is used for culture in vitro and detection of microorganisms in human blood or other sterile body fluid under normal condition.
Bi-state blood culture bottle is used for culture medium based qualitative detection of microorganisms in body fluids like blood
This kit is used for bacteria identification and 16 drugs susceptibility test for M.tuberculosis.
This kits is a rapid visual immunoassay for the qualitative
This reagent kit is used for the qualitative detection of fetal fibronectin (fFN) and insulin-like growth factor binding protein-1 (iGFBP-1) in human samples (vaginal secretions). It is primarily used in clinical settings as an adjunct for detecting preterm labor and premature rupture of membranes.
This test kit is used for the qualitative detection of transferrin in human stool samples. Clinically, it is primarily used to assess gastrointestinal bleeding and is for in vitro diagnostic use only.
This product uses antigen-antibody specific reaction and immunochromatographic analysis technology, and can qualitatively detect the presence of Helicobacter pylori antigen in stool without other supporting instruments.
This product is used for qualitative detection of Helicobacter pylori antibodies in serum.
This kit is suitable for qualitative detection of hemoglobin and transferrin in human fecal samples. It is mainly used in clinical assessment of gastrointestinal bleeding and only for in vitro diagnosis.
Intended use: For qualitative detection of rotavirus and/or adenovirus antigens in feces of infants and toddlers.
This kit is suitable for qualitative detection of hemoglobin in human faecal samples, and is mainly used clinically for evaluating gastrointestinal bleeding. In vitro diagnosis only.
This product is used for qualitative detection of group A rotavirus antigen in feces of infants and toddlers.
This product is mainly suitable for urogenital tract system ureaplasma Urealyticum (UU), Mycoplasma hominis (MH) for culture, identification, and determination of drug sensitivity.
This product is mainly suitable for mycoplasma culture colony confirmation.
This kit uses highly specific antibody-antigen reactions and immunochromatographic analysis technology to qualitatively detect the presence of Neisseria gonorrhoeae antigens in clinical reproductive tract specimens. It is suitable for rapid detection of gonorrhea and is especially useful for physical examinations or mass population screening.
For one-time use in the isolation and culture of Neisseria gonorrhoeae in medical units.
This product is mainly suitable for clinical isolation and culture of mycoplasma.
This product is mainly suitable for clinical isolation and culture of mycoplasma.
This product is primarily used for the isolation and cultivation of mycoplasma in clinical settings.
This kit is intended for use as an aid in the diagnosis of bacterial vaginosis.
Bacterial Vaginosis (BV) Test kit（Test） is for rapid diagnosis and treatment evaluation of bacterial vaginosis. This kit is intended for use as an aid in the diagnosis of bacterial vaginosis.
Bacterial Vaginosis Combo Test Kit is for rapid screening, diagnosis and treatment evaluation of Bacterial vaginosis.
Bacterial Vaginosis Combo Test Kit is for rapid screening, diagnosis and treatment evaluation of Bacterial vaginosis.
The Tuberculosis IgG Rapid Test Device (Serum/)is is one kind of immunochromatographic kit to detect M.
The Influenza A+B / COVID-19 / RSV Antigen Rapid Test Device is a rapid visual immunoassay for the qualitative, presumptive detection of influenza A and B viral antigens
The sample diluent is used to dilute and liquefy samples for testing with in vitro diagnostic reagents or instruments. Specifically, the phosphate buffer is used to neutralize digested sputum specimens and to resuspend precipitated specimens.
Phosphate Buffer Solution
Suitable for the transportation and storage of Mycobacterium strains, without affecting their growth.
Used for the collection, transportation, and storage of samples.
The sample dilution liquid is used to dilute and liquefy the sample for testing, facilitating the use of in vitro diagnostic reagents or instruments for analysis. Specifically, the Mycobacterium suspension preparation reagent is suitable for grinding, preparing, and diluting Mycobacterium suspensions.
Sample liquefyingagent is used to dilute and liquefy the sample for IVD or instrument test. Mycobacterial suspension preparation reagent is used to grind, bacterial suspension preparation and dilution.
Sample liquefyingagent is used to dilute and liquefy the sample for IVD or instrument test. NaOH alkali treatment liquid is applied to sputum sample mycobaterial or other non-aseptic liquid alkali direct treatment.
Sample liquefyingagent is used to dilute and liquefy the sample for IVD or instrument test. NALC Sputum digest is applied to sputum sample treatment before mybobaterial test.
The sample diluent is used to dilute and liquefy the sample to facilitate testing with in vitro diagnostic reagents or instruments. It does not participate directly in the detection process.
The sample diluent is used to dilute and liquefy the sample for testing with in vitro diagnostic reagents or instruments. The Mycobacterium suspension preparation reagent is specifically for the grinding, preparation, and dilution of Mycobacterium suspensions.
For determining the uniformity and consistency of bacterial suspensions.
0756-3983888
WeChat Official
Tuberculosis
No. 020, Honghui 2nd Road, Hongqi Industrial Zone, Jinwan District, Zhuhai City
0756-3983809
sales@encode.com.cn
